Works matching IS 08853185 AND DT 2013 AND VI 28 AND IP 6


Results: 41
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    The syndrome of deafness-dystonia: Clinical and genetic heterogeneity.

    Published in:
    Movement Disorders, 2013, v. 28, n. 6, p. 795, doi. 10.1002/mds.25394
    By:
    • Kojovic, Maja;
    • Pareés, Isabel;
    • Lampreia, Tania;
    • Pienczk‐Reclawowicz, Karolina;
    • Xiromerisiou, Georgia;
    • Rubio‐Agusti, Ignacio;
    • Kramberger, Milica;
    • Carecchio, Miryam;
    • Alazami, Anas M.;
    • Brancati, Francesco;
    • Slawek, Jaroslaw;
    • Pirtosek, Zvezdan;
    • Valente, Enza Maria;
    • Alkuraya, Fowzan S.;
    • Edwards, Mark J.;
    • Bhatia, Kailash P.
    Publication type:
    Article
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    Commentary.

    Published in:
    Movement Disorders, 2013, v. 28, n. 6, p. 739, doi. 10.1002/mds.25521
    By:
    • Foltynie, Thomas
    Publication type:
    Article
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    Primary progressive aphasia with parkinsonism.

    Published in:
    Movement Disorders, 2013, v. 28, n. 6, p. 741, doi. 10.1002/mds.25341
    By:
    • Doherty, Karen M.;
    • Rohrer, Jonathan D.;
    • Lees, Andrew J.;
    • Holton, Janice L.;
    • Warren, Jason
    Publication type:
    Article
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    Unusual DaTscan results.

    Published in:
    Movement Disorders, 2013, v. 28, n. 6, p. 847, doi. 10.1002/mds.25448
    By:
    • FuenteFernndez, Raúl
    Publication type:
    Article
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    Lysosomal impairment in Parkinson's disease.

    Published in:
    Movement Disorders, 2013, v. 28, n. 6, p. 725, doi. 10.1002/mds.25462
    By:
    • Dehay, Benjamin;
    • Martinez‐Vicente, Marta;
    • Caldwell, Guy A.;
    • Caldwell, Kim A.;
    • Yue, Zhenyue;
    • Cookson, Mark R.;
    • Klein, Christine;
    • Vila, Miquel;
    • Bezard, Erwan
    Publication type:
    Article
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    Alpha-synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease.

    Published in:
    Movement Disorders, 2013, v. 28, n. 6, p. 811, doi. 10.1002/mds.25421
    By:
    • Appel‐Cresswell, Silke;
    • Vilarino‐Guell, Carles;
    • Encarnacion, Mary;
    • Sherman, Holly;
    • Yu, Irene;
    • Shah, Brinda;
    • Weir, David;
    • Thompson, Christina;
    • Szu‐Tu, Chelsea;
    • Trinh, Joanne;
    • Aasly, Jan O.;
    • Rajput, Alex;
    • Rajput, Ali H.;
    • Stoessl, A.;
    • Farrer, Matthew J.
    Publication type:
    Article
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    Reply: Unusual DAT scan results.

    Published in:
    Movement Disorders, 2013, v. 28, n. 6, p. 847, doi. 10.1002/mds.25447
    By:
    • Ravina, Bernard;
    • Marek, Kenneth;
    • Eberly, Shirley;
    • Oakes, David;
    • Shoulson, Ira
    Publication type:
    Article
    40

    Movement Disorders in Adult Patients With Classical Galactosemia.

    Published in:
    Movement Disorders, 2013, v. 28, n. 6, p. 804, doi. 10.1002/mds.25348
    By:
    • Rubio‐Agusti, Ignacio;
    • Carecchio, Miryam;
    • Bhatia, Kailash P.;
    • Kojovic, Maja;
    • Parees, Isabel;
    • Chandrashekar, Hoskote S.;
    • Footitt, Emma J.;
    • Burke, Derek;
    • Edwards, Mark J.;
    • Lachmann, Robin H.L.;
    • Murphy, Elaine
    Publication type:
    Article
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